Variant #0000924963 (NC_000009.11:g.131019405A>G, NM_004408.2:c.*2412A>G (DNM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.131019405A>G
DNA change (hg38) -
Published as GOLGA2(NM_004486.6):c.2950T>C (p.C984R)
ISCN -
DB-ID CIZ1_000051
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 ?/. - c.*2412A>G r.(=) p.(=)
DNM1 NM_004408.2 ?/. - c.*2412A>G r.(=) p.(=)
GOLGA2 NM_004486.4 ?/. - c.2950T>C r.(?) p.(Cys984Arg)
CIZ1 NM_012127.2 ?/. - c.-52946T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.